Severe tooth wear in Prader-Willi syndrome. A case–control study

BACKGROUND: Prader-Willi syndrome (PWS) is a rare complex multsystemic genetic disorder characterized by severe neonatal hypotonia, endocrine disturbances, hyperphagia and obesity, mild mental retardation, learning disabilities, facial dysmorphology and oral abnormalities. The purpose of the present...

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Detalles Bibliográficos
Autores principales: Saeves, Ronnaug, Espelid, Ivar, Storhaug, Kari, Sandvik, Leiv, Nordgarden, Hilde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437195/
https://www.ncbi.nlm.nih.gov/pubmed/22639910
http://dx.doi.org/10.1186/1472-6831-12-12

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437195/
https://www.ncbi.nlm.nih.gov/pubmed/22639910
http://dx.doi.org/10.1186/1472-6831-12-12

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